Canonical Allele Identifier: CA631722534

Gene: C3

Linked Data

• gnomAD v2: 19-6709651-GT-G
• gnomAD v4: 19-6709640-GT-G
• MyVariant Identifiers: chr19:g.6709652del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709641del , CM000681.2:g.6709641del	GRCh38
NC_000019.9:g.6709652del , CM000681.1:g.6709652del	GRCh37
NC_000019.8:g.6660652del	NCBI36
NG_009557.1:g.16011del , LRG_27:g.16011del

Transcript Alleles

HGVS	Amino-acid change
ENST00000695652.1:c.1722+43del	ENSP00000512083.1:n.1722+43del
ENST00000695654.1:c.969+43del	ENSP00000512085.1:n.969+43del
ENST00000695655.1:c.786+43del	ENSP00000512086.1:n.786+43del
ENST00000695692.1:n.1209+43del
ENST00000245907.11:c.1845+43del MANE Select	ENSP00000245907.4:n.1845+43del
ENST00000245907.10:c.1845+43del	ENSP00000245907.4:n.1845+43del
NM_000064.3:c.1845+43del	NP_000055.2:n.1845+43del
NM_000064.4:c.1845+43del MANE Select	NP_000055.2:n.1845+43del